41. Searchalot Directory For Cleidocranial Dysplasia features. cleidocranial dysplasia Find information about this raregenetic disorder, chat and more topics for discussion. Baylor http://www.searchalot.com/Top/Health/ConditionsandDiseases/RareDisorders/Cleidoc

Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Rare Disorders : Cleidocranial Dysplasia Related Web Sites National Library of Medicine: CCD, CLCD - A list of synonyms of sleidocranial dysplasia, along with a summary and major features. Cleidocranial Dysplasia - Find information about this rare genetic disorder, chat and more topics for discussion. Baylor College of Medicine - An article entitled: A Natural History of Cleidocranial Dysplasia. MedicineNet.com: Medical Dictionary - An explanation of what cleidocranial dysplasia is and how it is transmitted. Readers Digest Health - Cleidocranial dysplasia, a list of alternate names, a general discussion and further resources.

42. Orthoguide.com Cleidocranial Dysplasia Search results for cleidocranial dysplasia . NO MATCHES FOUNDPlease select a differentkeyword or category OR Search AltaVista for 'cleidocranial dysplasia'. http://www.orthoguide.com/ortho/Cleidocranial_Dysplasia.php3

Search results for "Cleidocranial Dysplasia" NO MATCHES FOUND-Please select a different keyword or category OR Search AltaVista for 'Cleidocranial Dysplasia' Global Search Add Url Free Medline ... Search Enter Keywords to Search and Your Choice of Search Arguments Or And Match entire phrase Orthoguide.com

43. Health Library - Cleidocranial Dysplasia Saint Luke's Health System eLibrary. cleidocranial dysplasia. cleidocranial dysplasiais a rare craniofacial disorder inherited as an autosomal dominant trait. http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h

44. WebGuest - Open Directory Health Conditions And Diseases 941). Sites Baylor College of Medicine An article entitled A NaturalHistory of cleidocranial dysplasia. cleidocranial dysplasia http://directory.webguest.com/index.cgi/Health/Conditions_and_Diseases/Rare_Diso

45. Osteochondrodysplasias CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC; CHONDRODYSPLASIA, GREBETYPE. cleidocranial dysplasia Search PUBMED for Cleidocranial http://www.ohsu.edu/cliniweb/C5/C5.116.99.708.html

Osteochondrodysplasias Back to previous level Achondroplasia Search PUBMED for Achondroplasia: All Review Therapy Diagnosis ... Chondrodysplasia Punctata [1 more specific term/s, more link/s] Search PUBMED for Chondrodysplasia Punctata: All Review Therapy Diagnosis ... CHONDRODYSPLASIA, GREBE TYPE Cleidocranial Dysplasia Search PUBMED for Cleidocranial Dysplasia: All Review Therapy Diagnosis ... Cleidocranial Dysostosis: Med. Coll. of Wisconsin Diaphyseal Dysplasia, Progressive Search PUBMED for Diaphyseal Dysplasia, Progressive: All Review Therapy Diagnosis ... Camurati-Engelmann disease: Med. Coll. of Wisconsin Ellis-Van Creveld Syndrome Search PUBMED for Ellis-Van Creveld Syndrome: All Review Therapy Diagnosis ... Ellis-Van Creveld Syndrome: Med. Coll. of Wisconsin Enchondromatosis Search PUBMED for Enchondromatosis: All Review Therapy Diagnosis ... Fibrous Dysplasia of Bone [3 more specific term/s, 4 more link/s] Search PUBMED for Fibrous Dysplasia of Bone: All Review Therapy Diagnosis ... Fibrous Dysplasia: Med. Coll. of Wisconsin Hyperostosis, Cortical, Congenital Search PUBMED for Hyperostosis, Cortical, Congenital:

46. Craniofacial Abnormalities Craniofacial Abnormalities. Back to previous level cleidocranial dysplasiaSearch PUBMED for cleidocranial dysplasia All Review Therapy Diagnosis; http://www.ohsu.edu/cliniweb/C16/C16.131.621.207.html

Craniofacial Abnormalities Back to previous level Cleidocranial Dysplasia Search PUBMED for Cleidocranial Dysplasia: All Review Therapy Diagnosis ... Craniofacial Dysostosis [3 more specific term/s, 3 more link/s] Search PUBMED for Craniofacial Dysostosis: All Review Therapy Diagnosis ... Craniosynostoses [1 more specific term/s, 1 more link/s] Search PUBMED for Craniosynostoses: All Review Therapy Diagnosis ... Scaphocephaly: Med. Coll. of Wisconsin Holoprosencephaly Search PUBMED for Holoprosencephaly: All Review Therapy Diagnosis ... Maxillofacial Abnormalities [1 more specific term/s, more link/s] Search PUBMED for Maxillofacial Abnormalities: All Review Therapy Diagnosis Microcephaly Search PUBMED for Microcephaly: All Review Therapy Diagnosis Noonan Syndrome Search PUBMED for Noonan Syndrome: All Review Therapy Diagnosis Orofaciodigital Syndromes Search PUBMED for Orofaciodigital Syndromes: All Review Therapy Diagnosis ... OROFACIODIGITAL SYNDROME 1; OFD1 Platybasia Search PUBMED for Platybasia: All Review Therapy Diagnosis ... Basilar Invagination: Med. Coll. of Wisconsin Rubinstein-Taybi Syndrome Search PUBMED for Rubinstein-Taybi Syndrome: All Review Therapy Diagnosis ... KABUKI SYNDROME

47. Publications - Research Group Mundlos L, Lee PJ, Majewski F, Mulliken JB, Suri M, Zenker M, Mundlos S, Otto F. Mutationanalysis of core binding factor A1 in patients with cleidocranial dysplasia. http://www.molgen.mpg.de/research/mundlos/publications.html

home contact search Research Group Mundlos Publications Research Group Mundlos Projects Publications Team Publications Stricker S, Fundele R, Vortkamp A, Mundlos S Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 2002 May; 245,1: 98-108 Albrecht AN, Schwabe GC, Stricker S, Boddrich A, Wanker EE, Mundlos S. The synpolydactyly homolog (spdh) mutation in the mouse a defect in patterning and growth of limb cartilage elements. Mech Dev. 2002 Mar;112(1-2):53-67. Tiller GE, Hannig VL, Dozier D, Carrel L, Trevarthen KC, Wilcox WR, Mundlos S, Haines JL, Gedeon AK, Gecz J. A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda. Am J Hum Genet. 2001 Jun;68(6):1398-407. Nurnberg P, Thiele H, Chandler D, Hohne W, Cunningham ML, Ritter H, Leschik G, Uhlmann K, Mischung C, Harrop K, Goldblatt J, Borochowitz ZU, Kotzot D, Westermann F, Mundlos S, Braun HS, Laing N, Tinschert S. Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nat Genet.

48. Projects - Research Group Mundlos a number of previous studies mutations in CBFA1, a transcription factor from therunt family, were shown to be associated with cleidocranial dysplasia (CCD), a http://www.molgen.mpg.de/research/mundlos/projects.html

home contact search Research Group Mundlos Projects Research Group Mundlos Projects Publications Team Current projects Function of Cbfa1 (runx2) in osteoblast and chondrocyte differentiation Receptor tyrosine kinase Ror2 is mutated in Robinow syndrome and brachydactyly type B - molecular pathology and normal function Hoxd genes in limb development and cartilage differentiation Identification of genes regulated by Cbfa1 ... Receptor tyrosine kinase Ror2 is mutated in Robinow syndrome and brachydactyly type B - molecular pathology and normal function Brachydactyly is shortening of the digits due to abnormal development of the phalanges and/or metacarpals. It may occur as an isolated trait or as part of complex malformation syndromes. According to their patterns of skeletal involvement heritable brachydactylies have been classified into the subtypes A to E (Bell 1951). Autosomal dominant brachydactyly type B (BDB; MIM113000) is readily distinguished from other brachydactylies by the characteristic shortening/hypoplasia of the distal phalanges, the occurrences of nail dysplasia, hypoplasia of middle phalanges, and variable degrees of distal and proximal symphalangism. Broad thumbs with or without distal duplication/clefts and syndactyly can be additional findings. Robinow syndrome is a rare skeletal dysplasia with mesomelic shortening of the limbs, small stature, vertebral malformations and hypogenitalism. Both syndromes, brachydactyly type B as well as Robinow syndrome have been shown to be caused by mutations in ROR2. Our studies aim at the functional analysis of Ror2 during development.

49. Yunis Varon Syndrome HOME Yunis Varon Syndrome (cleidocranial dysplasia with Micrognathia,Absent Thumbs, and Distal Aphalangia). Yunis Varon Syndrome; http://www.bdid.com/yunisvaron.htm

HOME Yunis Varon Syndrome (Cleidocranial Dysplasia with Micrognathia, Absent Thumbs, and Distal Aphalangia) Yunis Varon Syndrome Yunis-Varon A child with YUNIS VARON SYNDROME Cleidocranial dysplasia micrognathia absent thumbs ... HOME

50. Directory :: Look.com cleidocranial dysplasia (6) See Also. Sites. Baylor College of MedicineAn article entitled A Natural History of cleidocranial dysplasia. http://www.look.com/searchroute/directorysearch.asp?p=523622

51. CancerGene CBFA1 Class, PUTATIVE ONCOGENE. Diseases, cleidocranial dysplasia. Otto F;Kanegane H;MundlosS Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. http://caroll.vjf.cnrs.fr/cancergene/CG505.html

Infobiogen Search CancerGene CancerGene Homepage Search CancerGene Citations CancerGene Card Symbol Aliases Name Core-binding factor alpha subunit 1; acute myeloid leukemia 3 gene Locus OMIM GDB SwissProt LocusLink Class PUTATIVE ONCOGENE Diseases Cleidocranial Dysplasia Note RUNX:A trilogy of cancer genes. (Lund and van Lohuizen, Cancer Cell, April 2002:1(3),213-215. Comments The t(8;21)(q22;q22) breakpoints on chromosome 21 in a cute m yeloid l eukemias are clustered within a limited region of a single gene, named AML1 by the authors (Miyoshi et al. 1991, UI:92073300 GenBank:D90525 CG:59 ). The product of AML1 has a region about 118 amino acids long that is highly homologous to the Drosophila segmentation gene runt (Daga et al. 1992, UI:92220161 ). Mouse homolog of the human AML1 is PEBP2alphaB ( p olyomavirus e nhancer b inding p rotein ), a runt domain gene, with 99% amino acid identity to the first 241 residues, including the runt homology region, of AML1 (Bae et al. 1993, UI:93173528 ). The runt domain identifies a family of heteromeric transcription regulators (reviewed by Kagoshima et al. 1993, UI:94098625 In studies aimed to elucidate the origin of transient leukemia in Down syndrome neonates Levanon et al. (1994

52. Cleidocranial Dysplasia: A Case Report cleidocranial dysplasia A Case Report. VictorB. Feldman, BSc, DC PDF Issue Index. http://www.ccachiro.org/client/cca/JCCA.nsf/Articles/1C661E4E907D9D8D85256C4E005

53. NORD - National Organization For Rare Disorders, Inc. cleidocranial dysplasia. To purchase fulltext report ($7.50) Copyright 1993,1995, 1996 Synonyms of cleidocranial dysplasia Cleidocranial Dysostosis; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Cleidocranial

54. Cleidocranial Dysostosis A Case Report Cleber Silva* ; Steven inversion of chromosome 6.13 It is also known as Marie and Sainton disease, mutationaldysostosis, craniocleido dysostosis and cleidocranial dysplasia.11 It http://cpmcnet.columbia.edu/dept/dental/Dental_Educational_Software/cdr97/silva.

Cleidocranial Dysostosis: A Case Report Cleber Silva* ; Steven DiRienzo, BS**; Neill Serman, DDS*** ABSTRACT The findings of cleidocranial dysostosis are reviewed. A case is presented where the clinical appearance of the patient should have made the clinician immediately aware of the possibility of the condition before performing an intraoral or radiographic examination. (Col Dent Rev 2:26, 1997) INTRODUCTION Cleidocranial dysostosis, CCD, is a rare developmental defect of autosomal dominant inheritance1,2, which has been mapped to a microdeletion of chromosome band 6p214, t(6;18) (p12;q24) translocation12 and pericentric inversion of chromosome 6.13 It is also known as Marie and Sainton disease, mutational dysostosis, craniocleido dysostosis and cleidocranial dysplasia.11 It presents with skeletal defects of several bones, the most striking of which is partial or complete absence of clavicles (Figure 1)1,3 and late closure of the fontanelles (which is also found in Basal Cell Nevus Syndrome and Crouzon Syndrome) resulting in frontal bossing. This condition is of clinical significance to the dentist due to the involvement of facial bones, altered eruption patterns, and presence of multiple supernumerary teeth.11 CASE REPORT A case is presented to show the importance of thorough observation of each patient's general appearance. A young mother in her late twenties (Figure 2) brought her asymptomatic, 12 year old daughter (Figure 3) into the dental clinic "for dental treatment". On intraoral examination, it was noted that the child had more primary teeth present than one would expect at this age, but not much thought was given to this finding at the initial examination (Figure 4). It was decided that panoramic and bitewing radiographs were required to evaluate the child's dentition.

55. WebMD - cleidocranial dysplasia Important It is possible that the main title ofthe report cleidocranial dysplasia is not the name you expected. http://my.webmd.com/NR/internal.asp?GUID={8BE0CC02-E2AB-4B02-A466-D3C7DFB793D0}

56. FSP Syndromes Normal Bladder; Sensation. Syringomyelia cleidocranial dysplasia.from A Kornberg MD. Familial syringomyelia with ArnoldChiari http://www.neuro.wustl.edu/neuromuscular/spinal/fsp.html

Front Search Index Links ... Patient Info FAMILIAL SPINAL CORD SYNDROMES General principles Familial Spastic Paraplegia ( SPG Dominant : Atlastin; 14q11 : Spastin; 2p22 SPG 12q Recessive : Paraplegin; 16q24 (Troyer): Spartin; 13q12.3 Infantile onset : Alsin; 2q33 X-linked : Proteolipid protein; Xq22 Other Familial Spastic Paraplegia +... Ataxia CNS Ocular PNS ... Systemic Disorders Leukodystrophies Adrenomyeloneuropathy : ALDP; Xq28 Adult-onset Krabbe : GalC; 14q31 MLD : Arylsulfatase A; 22q13 Other spinal cord syndromes Syndromes AAA syndrome : Aladin; 12q13 Adrenomyeloneuropathy : ALDP; Xq28 Alexander : GFAP; 17q21 Alzheimer's : Presenilin 1; 14q24 Arnold-Chiari Malformation Cavanagh's Cerebral palsy-Symmetrical Cerebrotendinous xanthomatosis : Cytochrome 450; 2q33 Charlevoix-Saguenay : Sacsin; 13q11 DOPA-responsive dystonias DRPLA : DRPLA protein; 12p13 Episodic ataxia Evans Fitzsimmons syndrome Friedreich ataxia : FRDA; 9q13 Hereditary Motor Syndromes HHH syndrome HMSN 5 : ARX; Xp22 Infections: HTLV-1 Krabbe : GalC; 14q31 L1 cell adhesion molecule (MASA) Lawrence-Moon Leukodystrophy: Adult-onset Mass lesions Mast syndrome Mental retardation Rett syndrome: Small testes : ATRX; Xq13

57. Maxillo Facial SHTEYER, Arie 4. cleidocranial dysplasia mapping and cloning of its gene in humans (collaborationwith Prof. A. Becker, Dr. A. Palmon, and Prof. J. Lustmann). http://www.hadassah.org.il/departments/maxilo_facial/shteyer.html

introduction staff Residency program Hadassah SHTEYER, Arie Born 1938, Kalish (Poland); D.M.D. 1964, Hebrew Univ.: Lect.1969; Sen.Lect.1973; Assoc.Prof.1978; Prof.1985; Dean, Faculty of Dental Medicine, 1990-1993. Head of the Department since 1996. Research Interests: Basic research : Purification of histone H4-related osteogenic growth peptide (OGP) from healing bone marrow; the effect of OGP on bone defects; the effect of OGP on osteoporosis; the effect of OGP on ridge augmentation; the effect of demineralized bone powder on osteoblast-like cells in culture and bone healing. Clinical research : The effect of slow-release antibiotics on post-extraction wounds in the jaw bones; anomalies in the facial skeleton; evaluation of dental implants. Cleidocranial Dysplasia: mapping and cloning the gene in humans. Distraction Osteogenesis of the Jaws Research Projects: 1. Osteogenic Growth Peptide derived from healing bone marrow (collaboration with Prof. I Bab, Prof. A. Muhlrad and Prof. M. Chorev).

58. Maxillo Facial Lustman Mapping and cloning the gene in humans affected by cleidocranial dysplasia. 1997.Becker, A., Lustmann, J., Shteyer, A. cleidocranial dysplasia. http://www.hadassah.org.il/departments/maxilo_facial/LUSTMANN_Joshua.html

introduction staff Residency program Hadassah LUSTMANN Joshua Born 1941, Poland. DMD - 1968, Hebrew Univ.: Lect.1975;Sen.Lect.1978;Assoc.Prof.1994. Research Interests and Research Projects: Impact of ArF excimer laser irradiation (193nm) on bone and its photoacoustic injury on bone cells and pulp tissue. Identification and initial characterization of oncogene involvement in Odontogenic Tumors. The possible involvement of the human T uftelin gene in Amelogenesis Imperfecta. Mapping and cloning the gene in humans affected by Cleidocranial Dysplasia. Developing new surg i cal techniques and their impact of implant surgery. Recent publications: Becker, A., Lustmann, J. and Shteyer, A.: Chapter 3 - Surgical exposure of impacted teeth. In: Becker, A. The orthodontic treatment of impacted teeth. London: Martin Dunitz Publishers. 1997 Becker, A., Lustmann, J., Shteyer, A.: Cleidocranial Dysplasia. Part I: General principles of the orthodontic and surgical treatment modality. Am J Orthod Dentofac Orthop Becker, A., Shteyer, A., Bimstein, E.

59. Otto Translate this page Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, isessential for osteoblast differentiation and bone development. http://www.ukl.uni-freiburg.de/med/med1/forschung/experimentell/projekte/mm1.htm

Molekulare Medizin I Arbeitsgebiet: Projektleiter: Dr. Florian Otto Email: otto@mm11.ukl.uni-freiburg.de Mitarbeiter: Dipl.-Biol. Michael Stock Cand. med. Jan-Henrik Eggers Ingrid Huber, MTA Malgorzata Gasperowicz, M.Sc. Projektbeschreibung: Die Differenzierungsvorgänge, durch die aus Stammzellen gewebsspezifische Zellen entstehen, werden durch spezifische Transkriptionsfaktoren reguliert. Unsere Arbeitsgruppe befasst sich mit einer Familie von Transkriptionsfaktoren (RUNX-Proteine), die u.a. die Differenzierung mesenchymaler Stammzellen zu reifen Osteoblasten sowie Differenzierungsvorgänge hämatopoetischer Stammzellen reguliert. Wir konnten in den vergangenen Jahren zeigen, dass RUNX2 für die Entstehung reifer Osteoblasten und somit für die Knochenbildung notwendig ist. Darüberhinaus konnten wir Mutationen im RUNX2-Gen als Ursache einer dominant erblichen Skelettfehlbildung des Menschen (Cleidocraniale Dysplasie) identifizieren. Die derzeit aktiven Projekte beschäftigen sich mit den folgenden Fragen: Welche Gene werden von RUNX2 transkriptionell reguliert?

60. Wheeless' Textbook Of Orthopaedics See Deformities of the Limbs Achondroplasia Chondrodysplasia Punctata ChondroectodermalDysplasia cleidocranial dysplasia Diastrophic Dwarfism http://wheeless.orthoweb.be/o14/91.htm

Main Menu Home Page Dwarfism and Dysplasias: - See: Deformities of the Limbs Achondroplasia Chondrodysplasia Punctata: Chondroectodermal Dysplasia ... Spondyloepiphyseal Dysplasia Congenita - Short Trunk Dwarfism: Kniest syndrome Metatrophic Dysplasia Spondyloepiphyseal dysplasias - Proportionate Dwarism: diastrophic dysplasia cleidocranial dysplasia dysplasia - mucopolysaccaridoses - Disproportionate dwarfism: (short limb dysplasia) Achondroplasia metaphyseal chondrodysplasias ; Rhizomelic Dwarfism: Arms or Thighs are Short relative to the entire limb Mesomelic Dwarfism: Disproportionately Short Forearms or Legs Acromelic Dwarfism: Disproportionately short hands or feet -

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